FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SUMO GLASS IONOMER CEMENT

K Number: K913519 · Decision Nov 19, 1991
Classifications
1
FEI Numbers
144
Registration Numbers
144
Same Product Code
504
Applicant Total
9
Review Days
104

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Basic Information

Device Name
SUMO GLASS IONOMER CEMENT
K Number
K913519
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3275
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ortho Source
Date Received
August 7, 1991
Decision Date
November 19, 1991
Product Code
EMA
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EMA Cement, Dental

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Other Clearances by Ortho Source

K Number Device Name
K913853 FISSURE SEALER
K913854 ORTHO LIGHT CURE
K884949 VISIBLE LIGHT CURE CALCIUM HYDROXIDE LINER
K884575 MAXIBOND
K861118 ORTHOJOIN, ORTHODONTIC ADHESIVE
K861258 PERMABAND (ORTHODONTIC ADHESIVE)
K861245 ORTHOSOURCE ETCH SYSTEMS
K860959 DEPENDABOND